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ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932857
510(k) Type
Traditional
Applicant
ANSLEY MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1993
Days to Decision
95 days
Submission Type
Statement

ABDOMINAL FLUID CONTROL POUCH, 203-301-S;ETC.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932857
510(k) Type
Traditional
Applicant
ANSLEY MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1993
Days to Decision
95 days
Submission Type
Statement